Electrophilic phenoxy-substituted phosphonium cations.

Dalton Trans

Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario, CanadaM5S 3H6.

Published: November 2016

A family of electrophilic phenoxy-substituted phosphonium salts [(RO)P(CF)][B(CF)] (R = CH, 4-FCH, 2,4-FCH, CF) have been synthesized and their air stability was evaluated. Computations of the fluoride ion affinity and global electrophilicity index have been used to compare the electrophilicity of these phosphonium salts. The Lewis acidity of these phosphonium salts was probed computationally and experimentally in a Friedel-Crafts-type dimerization, hydrodefluorination, hydrosilylation, hydrodeoxygenation, and dehydrocoupling reactions.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c6dt03544bDOI Listing

Publication Analysis

Top Keywords

phosphonium salts
12
electrophilic phenoxy-substituted
8
phenoxy-substituted phosphonium
8
phosphonium
4
phosphonium cations
4
cations family
4
family electrophilic
4
salts [ropcf][bcf]
4
[ropcf][bcf] 4-fch
4
4-fch 24-fch
4

Similar Publications

Pyridines can be deuterated at the remote sites by treatment with KOBu in DMSO- , although without discrimination between the - and -position. Herein, base-catalyzed deuterations have been studied, computationally and experimentally, using a series of pyridyl phosphonium salts with a temporary electron-withdrawing group to block the -position while increasing the acidity in the other positions.

View Article and Find Full Text PDF

Nucleophilic Functionalization of Activated P in [CpFe(CO)-(η-P)][Al(OR)] with Alcohols R-OH.

Chemistry

January 2025

Institut für Anorganische und Analytische Chemie and Freiburger Materialforschungszentrum (FMF), Universität Freiburg, Albertstr. 21, 79104, Freiburg, Germany.

The bonding situation in [Fp-P][Al(OR)] (1) (Fp = (CO)CpFe, R = C(CF)) gives rise to an Umpolung of the P fragment, which should make it accessible for nucleophiles. To investigate this projected reactivity, the complex was combined with a series of hydroxy-nucleophiles - that all do not react with free P - leading to a variety of P building blocks. With excess of R-OH (R = Me, Et, Ph), the thermodynamically more stable complex salts [Fp-P(H)(OR))][Al(OR)] (x=2,1,0) (2b-2d) are formed and show that the phosphonium type pathway is accessible.

View Article and Find Full Text PDF

(1) Background: Since the discovery of antibiotics in the first half of the 20th century, humans have abused this privilege, giving rise to antibiotic-resistant pathogens. Recent research has brought to light the use of antimicrobial peptides in polymers, hydrogels, and nanoparticles (NPs) as a newer and safer alternative to traditional antibiotics. (2) Methods: This review article is a synthesis of the scientific works published in the last 15 years, focusing on the synthesis of polymers with proven antimicrobial properties.

View Article and Find Full Text PDF

Advances in Pyridine C-H Functionalizations: Beyond C2 Selectivity.

Chemistry

January 2025

Department: Photocatalysis & Synthetic Methodology Lab (PSML), Amity Institute of Click Chemistry Research & Studies (AICCRS), Amity University, Noida, 201303, India.

Article Synopsis
  • The pyridine core is vital in many FDA-approved drugs and EPA-regulated chemicals, serving as a key structural component in various applications like ligands and catalysts.
  • Direct functionalization of pyridine is challenging due to its unstable nature and nitrogen's strong coordination, but recent advancements in regioselective C-H activation techniques show promise for improving this process.
  • This review highlights innovative strategies for meta and para-C-H functionalization, discussing both their advantages and limitations, to encourage further developments in pyridine chemistry.
View Article and Find Full Text PDF

By strategic design and synthesis of a new series of phosphonium salts (compounds 1-7[OTf]), where [OTf] stands for the trifluoromethanesulfonate anion, we performed comprehensive spectroscopic and dynamic studies on the photoinduced anion migration in toluene. Our aim is to probe if the anion migration is associated with an intrinsic barrier or is barrier-free. After the occurrence of excited-state intramolecular charge transfer (ESICT) in 1-7, the charge redistribution of the cation triggers the translocation of the counter anion [OTf], resulting in emission spectral temporal evolution.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!